Neurons and satellite glial cells in adult rat lumbar dorsal root ganglia express connexin 36

被引:13
作者
Perez Armendariz, E. Martha [1 ]
Norcini, Monica [2 ]
Hernandez-Tellez, Beatriz [1 ]
Caste-Rodriguez, Andres [1 ]
Coronel-Cruz, Cristina [1 ]
Guerrero Alquicira, Raquel [1 ]
Sideris, Alexandra [2 ]
Recio-Pinto, Esperanza [2 ,3 ,4 ]
机构
[1] Univ Nacl Autonoma Mexico, Dept Biol Celular & Tisular, Fac Med, Torre Invest 5to Piso,Ave Univ 3000,Ciudad Univ, Mexico City 04510, DF, Mexico
[2] NYULMC, Dept Anesthesiol, 180 Varick St,Room 677, New York, NY 10014 USA
[3] NYULMC, Dept Biochem, 180 Varick St,Room 677, New York, NY 10014 USA
[4] NYULMC, Dept Mol Pharmacol, 180 Varick St,Room 677, New York, NY 10014 USA
关键词
Connexin; 36; Cx36; Dorsal root ganglia; Satellite glial cells; Primary sensory neurons; Spared nerve injury; PRIMARY SENSORY NEURONS; DIMORPHIC MOTOR NUCLEI; GAP-JUNCTION CHANNELS; SPINAL-CORD; ELECTRICAL SYNAPSES; NEUROPATHIC PAIN; ANIMAL-MODEL; MOUSE; BETA; MOTONEURONS;
D O I
10.1016/j.acthis.2017.11.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Previous studies have shown that following peripheral nerve injury there was a downregulation of the gap junction protein connexin 36 (Cx36) in the spinal cord; however, it is not known whether Cx36 protein is expressed in the dorsal root ganglia (DRGs), nor if its levels are altered following peripheral nerve injuries. Here we address these aspects in the adult rat lumbar DRG. Cx36 mRNA was detected using qRT-PCR, and Cx36 protein was identified in DRG sections using immunohistochemistry (IHC) and immunofluorescence (IF). Double staining revealed that Cx36 co-localizes with both anti-beta-III tubulin, a neuronal marker, and anti-glutamine synthetase, a satellite glial cell (SGC) marker. In neurons, Cx36 staining was mostly uniform in somata and fibers of all sizes and its intensity increased at the cell membranes. This labeling pattern was in contrast with Cx36 IF dots mainly found at junctional membranes in islet beta cells used as a control tissue. Co-staining with anti-Cx43 and anti-Cx36 showed that whereas mostly uniform staining of Cx36 was found throughout neurons and SGCs, Cx43 IF puncta were localized to SGCs. Cx36 mRNA was expressed in normal lumbar DRG, and it was significantly down-regulated in L4 DRG of rats that underwent sciatic nerve injury resulting in persistent hypersensitivity. Collectively, these findings demonstrated that neurons and SGCs express Cx36 protein in normal DRG, and suggested that perturbation of Cx36 levels may contribute to chronic neuropathic pain resulting from a peripheral nerve injury.
引用
收藏
页码:168 / 178
页数:11
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